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82722-74-5

4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois a heterocyclic chemical compound with the molecular formula C9H7N3O3. It features a unique structure that includes nitrogen and oxygen atoms, and is characterized by the presence of a nitro group. 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois a derivative of nitroimidazoles, which are known for their potential antimicrobial and antitumor properties. Its distinctive chemical properties and potential applications in medicinal chemistry make it a significant subject of research for the development of pharmaceutical drugs and new treatments for various diseases.

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  • 82722-74-5 Structure

  • Basic information

    1. Product Name: 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-
    2. Synonyms: 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-;3,5-dihydro-7-nitro-4H-Imidazo[4,5-c]pyridin-4-one
    3. CAS NO:82722-74-5
    4. Molecular Formula: C6H4N4O3
    5. Molecular Weight: 180.12096
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82722-74-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-(82722-74-5)
    11. EPA Substance Registry System: 4H-IMidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-(82722-74-5)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 82722-74-5(Hazardous Substances Data)

82722-74-5 Usage

Uses

Used in Pharmaceutical Development:
4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois used as a key intermediate in the synthesis of pharmaceutical drugs for its potential antimicrobial and antitumor properties. Its unique structure allows for the development of new compounds that can target specific diseases and conditions.
Used in Antimicrobial Applications:
In the field of antimicrobial research, 4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois utilized as a precursor for the creation of new antimicrobial agents. Its nitro group is known to contribute to the effectiveness against various types of bacteria and other microorganisms, making it a valuable component in the fight against antibiotic-resistant strains.
Used in Antitumor Research:
4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois also used in antitumor research, where it serves as a building block for the development of new cancer treatments. Its potential to target and affect tumor cells makes it a promising candidate for further investigation and development in oncology.
Used in Medicinal Chemistry Research:
In the broader field of medicinal chemistry, 4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitrois employed as a subject of study to understand its chemical properties and how they can be harnessed for therapeutic purposes. This includes exploring its reactivity, stability, and interactions with biological systems to enhance drug design and discovery.

Check Digit Verification of cas no

The CAS Registry Mumber 82722-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,7,2 and 2 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82722-74:
(7*8)+(6*2)+(5*7)+(4*2)+(3*2)+(2*7)+(1*4)=135
135 % 10 = 5
So 82722-74-5 is a valid CAS Registry Number.

82722-74-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4H-Imidazo[4,5-c]pyridin-4-one, 3,5-dihydro-7-nitro-

1.2 Other means of identification

Product number -
Other names 7-Nitro-1H-imidazo[4,5-c]pyridin-4(5H)-one

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:82722-74-5 SDS

82722-74-5Downstream Products

82722-74-5Relevant articles and documents

3-nifro-3-deaza-2′-deoxyadenosine as a versatile photocleavable 2′-deoxyadenosine mimic

Crey-Desbiolles, Caroline,Lhomme, Jean,Dumy, Pascal,Kotera, Mitsuharu

, p. 9532 - 9533 (2007/10/03)

A new photocleavable 2′-deoxyadenosine mimic, 3-nitro-3-deaza-2′-deoxyadenosine (NidA), was prepared and introduced into DNA fragments via its 6-O-trimethylphenyl precursor phophoramidite. Photocleavage of the resulting oligonucleotide is highly efficient

Synthesis and Some Reactions of 7-Nitroimidazo[4,5-c]pyridin-4-ones

Yutilov, Yu. M.,Svertilova, I. A.

, p. 451 - 455 (2007/10/03)

Imidazo[4,5-c]pyridin-4-one and its alkyl-substituted derivatives are readily nitrated under mild conditions to give the corresponding 7-nitro derivatives. The position of the nitro group is confirmed by comparison of the 1H NMR spectra of the nitration products of imidazo[4,5-c]pyridin-4-one and its deuterated analog. Some transformations of the resulting nitro compounds through the carbonyl group have been studied.

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